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雌激素受体α阴性子宫内膜癌中GATA3的表达可识别具有高增殖性和患者生存率低的侵袭性肿瘤。

GATA3 expression in estrogen receptor alpha-negative endometrial carcinomas identifies aggressive tumors with high proliferation and poor patient survival.

作者信息

Engelsen Ingeborg B, Stefansson Ingunn M, Akslen Lars A, Salvesen Helga B

机构信息

Department of Obstetrics and Gynecology, Haukeland University Hospital, Bergen, Norway.

出版信息

Am J Obstet Gynecol. 2008 Nov;199(5):543.e1-7. doi: 10.1016/j.ajog.2008.04.043. Epub 2008 Jul 3.

Abstract

OBJECTIVE

The transcription factor GATA3 has recently been found to be involved in the carcinogenesis for numerous cancers. We investigated this marker in relation to clinicopathologic characteristics, hormone receptors, other biomarkers, and survival in endometrial carcinoma.

STUDY DESIGN

A population-based study of 316 endometrial carcinomas with complete follow-up was studied for GATA3, estrogen receptor (ER)-alpha, ERbeta2, and progesterone receptor (PR) expression.

RESULTS

Positive GATA3 expression in hysterectomy specimens significantly correlated to high International Federation of Gynecology and Obstetrics stage, serous papillary/clear cell subtypes, high histologic grade, loss of PR expression, aneuploidy, high proliferation, pathologic p53 and p16 expression, and poor prognosis (P = .003). Loss of hormone receptors significantly correlated with aggressive phenotype and poor prognosis. Pathologic expression of GATA3/ERalpha in combination added independent prognostic information.

CONCLUSION

GATA3 expression is associated with an aggressive phenotype and adds independent prognostic information in addition to receptor status. Further studies of its value in tailored treatment protocols seem justified.

摘要

目的

转录因子GATA3最近被发现与多种癌症的致癌作用有关。我们研究了该标志物与子宫内膜癌的临床病理特征、激素受体、其他生物标志物及生存率的关系。

研究设计

对316例有完整随访资料的子宫内膜癌进行基于人群的研究,检测GATA3、雌激素受体(ER)α、ERβ2和孕激素受体(PR)的表达。

结果

子宫切除标本中GATA3阳性表达与国际妇产科联盟(FIGO)高分期、浆液性乳头状/透明细胞亚型、高组织学分级、PR表达缺失、非整倍体、高增殖率、病理p53和p16表达以及预后不良显著相关(P = 0.003)。激素受体缺失与侵袭性表型和预后不良显著相关。GATA3/ERα的病理表达联合可提供独立的预后信息。

结论

GATA3表达与侵袭性表型相关,除受体状态外还可提供独立的预后信息。进一步研究其在个性化治疗方案中的价值似乎是合理的。

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